# Simultaneous Gastric Cancer Metastases to the Small and Large Intestines: Hidden Small Intestinal Lesions and Colonic-Mimicking Metastases

**Authors:** Sota Nakamura, Manabu Yamamoto, Tsukasa Nakamura, Yuki Tateishi, Ryo Sakada, Shoichiro Nagashima, Kazutoyo Morita, Hidefumi Higashi, Tomoharu Yoshizumi

PMC · DOI: 10.70352/scrj.cr.25-0158 · 2025-10-28

## TL;DR

A rare case of gastric cancer spreading to both the small and large intestines is described, highlighting the importance of accurate diagnosis to avoid misinterpretation as separate intestinal cancers.

## Contribution

This case report highlights the diagnostic challenge of simultaneous gastric cancer metastases to both small and large intestines, emphasizing the role of immunohistochemistry in confirming metastatic origin.

## Key findings

- Simultaneous metastases to both small and large intestines from gastric cancer are extremely rare and may mimic synchronous primary intestinal cancers.
- Immunohistochemical markers (CK7, CK20, CDX2, SATB2, Arginase-1) helped confirm metastatic origin rather than primary colorectal cancer.
- Preoperative and intraoperative imaging may miss rare metastatic patterns, necessitating histopathological analysis for accurate diagnosis.

## Abstract

Gastric cancer often presents with metastases at diagnosis, but simultaneous metastases to both the small and large intestines are extremely rare and may be misinterpreted as synchronous primary intestinal cancers, particularly when preoperative imaging is inconclusive.

A 78-year-old male receiving cabozantinib for hepatocellular carcinoma with vertebral metastasis presented with anorexia, epigastric discomfort, and melena. Endoscopy revealed an ulcerative gastric lesion, and colonoscopy showed irregular ulcerative lesions in the ascending and transverse colons. The patient underwent laparoscopic distal gastrectomy, right hemicolectomy. During surgery, a small intestinal tumor was suspected, prompting an additional partial resection. Histopathology and immunohistochemistry (CK7, CK20, CDX2, SATB2, Arginase-1) confirmed that the intestinal lesions were metastases from gastric cancer rather than synchronous primary colorectal cancers.

This case suggests that preoperative and intraoperative imaging may not detect rare metastatic patterns, and that immunohistochemical analysis may help estimate tumor origin. Careful differentiation between true synchronous colorectal cancer and gastric cancer with intestinal metastases may help guide treatment decisions.

## Linked entities

- **Proteins:** KRT7 (keratin 7), KRT20 (keratin 20), CDX2 (caudal type homeobox 2), SATB2 (SATB homeobox 2), Arg1 (arginase 1)
- **Chemicals:** cabozantinib (PubChem CID 25102847)
- **Diseases:** gastric cancer (MONDO:0001056), hepatocellular carcinoma (MONDO:0007256)

## Full-text entities

- **Genes:** KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}, ARG1 (arginase 1) [NCBI Gene 383], KRT7 (keratin 7) [NCBI Gene 3855] {aka CK7, K2C7, K7, SCL}, CDX2 (caudal type homeobox 2) [NCBI Gene 1045] {aka CDX-3, CDX2/AS, CDX3}, SATB2 (SATB homeobox 2) [NCBI Gene 23314] {aka C2DELq32q33, DEL2Q32Q33, GLSS}
- **Diseases:** Metastases (MESH:D009362), ulcerative lesions (MESH:D014456), epigastric discomfort (MESH:C537170), colorectal cancer (MESH:D015179), tumor (MESH:D009369), intestinal cancers (MESH:D007414), Gastric Cancer (MESH:D013274), ulcerative gastric lesion (MESH:D013276), hepatocellular carcinoma (MESH:D006528), anorexia (MESH:D000855), Intestinal Lesions (MESH:D007410), melena (MESH:D008551)
- **Chemicals:** cabozantinib (MESH:C558660)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12558711/full.md

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Source: https://tomesphere.com/paper/PMC12558711